Yuvaraj Bhoobalan-Chitty1§
, Xiaoxiao Duan1, and Xu Peng1
1Department of Biology, University of Copenhagen, Copenhagen N, Denmark
§Correspondence to: Yuvaraj Bhoobalan-Chitty (yuvarajb@bio.ku.dk)
Abstract
Description
Methods
Reagents
Extended Data
- Description: List of spacer sequences newly acquired upon infection with SIRV2M (column 1) and their PAM sequence (column 2). The CRISPR-Cas subtypes capable of utilizing each new spacer is specified (column 3) along with the location of the spacer in the SIRV2 genome (column 4). Spacer complementarity to sense strand (column 1) is especially important for the transcription dependent targeting of subtype III-B CRISPR-Cas systems.. Resource Type: Text. DOI: 10.22002/che7n-2dw90
Acknowledgements
Funding
Author Contributions
- Yuvaraj Bhoobalan-Chitty: Conceptualization, Investigation, Methodology, Data curation, Funding acquisition, Visualization, Writing - original draft
- Xiaoxiao Duan: Investigation
- Xu Peng: Conceptualization, Funding acquisition, Writing - review & editing
Reviewed By
Susanne Erdmann
History
- Received: 10/16/2022
- Revision Received: 11/6/2022
- Accepted: 11/8/2022
- Published Online: 11/8/2022
- Indexed: 11/22/2022
Copyright
© 2022 by the authors. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International (CC BY 4.0) License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation
PubMed Central: 9682418
PubMed: 36439395
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